Variant report

Variant	rs1935526
Chromosome Location	chr6:73641447-73641448
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:73635330..73637431-chr6:73640282..73642642,2	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10805969	0.85[AMR][1000 genomes]
rs11756197	0.83[JPT][hapmap];0.86[AMR][1000 genomes]
rs12526735	0.81[JPT][hapmap]
rs12664704	0.84[CHB][hapmap]
rs1316784	1.00[CEU][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1342337	1.00[CEU][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17800259	0.84[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.86[AMR][1000 genomes]
rs1891396	0.87[CHD][hapmap]
rs1935527	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2882328	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2995346	0.84[CHB][hapmap]
rs3005769	0.84[CHB][hapmap];0.90[CHD][hapmap]
rs3763159	0.84[CHB][hapmap];0.89[CHD][hapmap]
rs4388257	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4552693	1.00[CEU][hapmap];0.82[CHB][hapmap];0.84[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6908756	0.83[CHB][hapmap];0.82[JPT][hapmap];0.85[AMR][1000 genomes]
rs6909147	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6909225	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6909241	0.84[CHB][hapmap];0.86[AMR][1000 genomes]
rs6913925	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6915633	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6916116	0.82[ASW][hapmap];0.91[LWK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs6924175	0.81[AMR][1000 genomes]
rs6924280	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929515	0.89[ASW][hapmap];0.95[CEU][hapmap];0.94[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6930157	0.84[CHB][hapmap];0.86[CHD][hapmap];0.85[GIH][hapmap];0.84[MEX][hapmap];0.87[TSI][hapmap];0.85[AMR][1000 genomes]
rs71573567	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7740837	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9341390	1.00[CEU][hapmap];0.84[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9342981	0.84[CHB][hapmap]
rs9342986	0.95[CEU][hapmap];0.89[CHB][hapmap];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9342987	1.00[CEU][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9351950	0.84[CHB][hapmap];0.90[CHD][hapmap]
rs9351951	0.84[CHB][hapmap];0.90[CHD][hapmap]
rs9351954	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9351955	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9351956	0.89[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9360608	0.83[CHB][hapmap]
rs9360610	0.84[CHB][hapmap];0.86[CHD][hapmap];0.85[GIH][hapmap];0.84[JPT][hapmap];0.87[TSI][hapmap];0.86[AMR][1000 genomes]
rs9360611	0.84[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.86[AMR][1000 genomes]
rs9360612	0.83[CEU][hapmap];0.84[CHB][hapmap];0.89[AMR][1000 genomes]
rs9360614	0.91[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9360616	0.87[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9360617	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9360618	1.00[CEU][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9360619	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830691	chr6:73530978-73743648	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
2	nsv886155	chr6:73551937-73649330	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1935526	SMAP1	cis	parietal	SCAN

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73607600-73715400	Weak transcription	Primary B cells from cord blood	blood
2	chr6:73624600-73658600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr6:73630000-73648400	Weak transcription	Aorta	Aorta
4	chr6:73641200-73641800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr6:73641200-73641800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:73641200-73642000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:73641200-73642000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr6:73641200-73642000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr6:73641200-73642200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:73641200-73642200	Enhancers	Fetal Brain Male	brain
11	chr6:73641200-73642200	Enhancers	Fetal Heart	heart
12	chr6:73641400-73641600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:73641400-73641800	Enhancers	Psoas Muscle	Psoas
14	chr6:73641400-73642000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:73641400-73642000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr6:73641400-73642200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr6:73641400-73642200	Enhancers	Fetal Brain Female	brain

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